MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH
K-Number: K760785 · 1976-11-01
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Device Summary
Frequently Asked Questions
What is the MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH?
MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Heyer Schulte Corp.. The 510(k) number is K760785.
When did MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH receive FDA 510(k) clearance?
MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760785.
Who is the listed applicant for MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH?
The FDA 510(k) record lists Heyer Schulte Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH?
The FDA product code for MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH is JXG.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Heyer Schulte Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JXG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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